Canonical Allele Identifier: CA399727261

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152676A>T (hg19) ; chr17:g.44075308A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075308A>T , CM000679.2:g.44075308A>T	GRCh38
NC_000017.10:g.42152676A>T , CM000679.1:g.42152676A>T	GRCh37
NC_000017.9:g.39508202A>T	NCBI36
NG_015818.1:g.9579A>T , LRG_182:g.9579A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*373-2A>T	ENSP00000466983.1:n.*373-2A>T
ENST00000588558.6:c.*511-2A>T	ENSP00000467624.1:n.*511-2A>T
ENST00000590253.3:c.417-2A>T	ENSP00000465111.2:n.417-2A>T
ENST00000593115.2:c.*557-2A>T	ENSP00000466821.1:n.*557-2A>T
ENST00000696383.1:c.191-2A>T	ENSP00000512593.1:n.191-2A>T
ENST00000696384.1:c.*96-2A>T	ENSP00000512594.1:n.*96-2A>T
ENST00000696385.1:c.*254-2A>T	ENSP00000512595.1:n.*254-2A>T
ENST00000696386.1:c.219-2A>T	ENSP00000512596.1:n.219-2A>T
ENST00000696387.1:c.*163-2A>T	ENSP00000512597.1:n.*163-2A>T
ENST00000696388.1:c.*382-2A>T	ENSP00000512598.1:n.*382-2A>T
ENST00000696389.1:c.*567-2A>T	ENSP00000512599.1:n.*567-2A>T
ENST00000696390.1:c.326-2A>T	ENSP00000512600.1:n.326-2A>T
ENST00000696391.1:c.*392-2A>T	ENSP00000512601.1:n.*392-2A>T
ENST00000696392.1:c.536-2A>T	ENSP00000512602.1:n.536-2A>T
ENST00000696393.1:c.536-2A>T	ENSP00000512603.1:n.536-2A>T
ENST00000696405.1:c.536-2A>T	ENSP00000512607.1:n.536-2A>T
ENST00000269097.9:c.536-2A>T MANE Select	ENSP00000269097.3:n.536-2A>T
ENST00000269097.8:c.536-2A>T	ENSP00000269097.3:n.536-2A>T
ENST00000585361.5:c.*373-2A>T	ENSP00000466983.1:n.*373-2A>T
ENST00000588558.5:c.*511-2A>T	ENSP00000467624.1:n.*511-2A>T
ENST00000590253.2:c.38-2A>T
ENST00000590639.1:n.555A>T
ENST00000591696.1:c.428-2A>T	ENSP00000468677.1:n.428-2A>T
NM_138387.3:c.536-2A>T , LRG_182t1:c.536-2A>T	NP_612396.1:n.536-2A>T
NR_028581.1:n.966-2A>T
NR_028582.1:n.831-2A>T
XM_006722179.2:c.417-2A>T	XP_006722242.1:n.417-2A>T
XM_011525473.1:c.191-2A>T	XP_011523775.1:n.191-2A>T
XM_011525474.1:c.191-2A>T	XP_011523776.1:n.191-2A>T
NM_001319945.1:c.417-2A>T	NP_001306874.1:n.417-2A>T
XM_011525473.3:c.191-2A>T	XP_011523775.1:n.191-2A>T
XM_011525474.3:c.191-2A>T	XP_011523776.1:n.191-2A>T
XM_017025335.2:c.191-2A>T	XP_016880824.1:n.191-2A>T
NM_001319945.2:c.417-2A>T	NP_001306874.1:n.417-2A>T
NR_028581.2:n.785-2A>T
NR_028582.2:n.650-2A>T
NM_001384165.1:c.191-2A>T	NP_001371094.1:n.191-2A>T
NM_001384166.1:c.191-2A>T	NP_001371095.1:n.191-2A>T
NM_001384167.1:c.191-2A>T	NP_001371096.1:n.191-2A>T
NM_001384168.1:c.191-2A>T	NP_001371097.1:n.191-2A>T
NM_138387.4:c.536-2A>T MANE Select	NP_612396.1:n.536-2A>T